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The effect of intravenous patient-controlled analgesia with oxycodone or sufentanil on postoperative recovery in patients undergoing knee arthroscopic surgery: A randomized controlled clinical trial

The effect of intravenous patient-controlled analgesia with oxycodone or sufentanil on postoperative recovery in patients undergoing knee arthroscopic surgery: A randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500112696
Enrollment
Unknown
Registered
2025-11-18
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee arthroscopy

Interventions

Group O:30 minutes before the end of surgery, administer an intravenous injection of oliceridine 1.5 mg and ondansetron 4 mg. Immediately after entering the PACU, perform PCIA, prepare the analgesia p
Group S:30 minutes before the end of surgery, 7.5 ug of sufentanil and 4 mg of ondansetron were administered intravenously. Immediately after entering the PACU, PCIA was performed, and the analgesic p

Sponsors

Longhua District People's Hospital, Shenzhen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years; 2. ASA classification I - III; 3. Understand and sign the informed consent; 4. Planned elective knee arthroscopic surgery; 5. BMI 18-28 kg/m^2.

Exclusion criteria

Exclusion criteria: 1. Individuals with severe cardiopulmonary dysfunction. 2. Individuals with abnormal electrocardiograms (e.g., prolonged QT interval). 3. Individuals with neurological or psychiatric disorders or a history thereof. 4. Patients with chronic pain, neuropathic pain, or a history of long-term analgesic use and alcohol abuse. 5. History of opioid allergy. 6. Use of medications that may affect analgesic response (central alpha-adrenergic agonists, antiepileptic drugs, nerve stimulants, antidepressants, or antipsychotics), without a fixed dose administered >=30 days preoperatively. 7. Recent receipt of other related surgeries that may affect study results.

Design outcomes

Primary

MeasureTime frame
Postoperative recovery quality;The occurrence of perioperative adverse events;The use of remedial drugs;The effective number of compressions of the analgesic pump and the total number of compressions;

Secondary

MeasureTime frame
Postoperative recovery quality;Pain score;

Countries

China

Contacts

Public ContactKuang Xin

People's Hospital of Longhua District, Shenzhen, Guangdong Province

kx6924@126.com+86 136 8499 6516

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026